“…This may be explained by complicated transfer of lithium ion species inside the electrode layer due to a variation in the pore structure after calendering. It is known that a high compression rate of the electrode reduces its porosity resulting in poorer wettability by an electrolyte . At the same time, an increase in the roll temperature results in both better C‐rate performance and cycling stability, which may be associated with becoming PVDF more flexible at higher temperature and, as a result, improvement the adhesion strength and electrical interface between cathode layer and current collector .…”